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Search Thermo Fisher Scientific
AATGGCGCTGGCCGCTCGTTTGCTA[C/T]CCCAGTTCCTGCACTCTCGGTCGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C2orf47 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
C2orf47 - chromosome 2 open reading frame 47 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024520.2 | 258 | Missense Mutation | CCC,TCC | P,S 9 | NP_078796.2 | |
XM_005246852.2 | 258 | Missense Mutation | CCC,TCC | P,S 9 | XP_005246909.1 |
TYW5 - tRNA-yW synthesizing protein 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039693.2 | 258 | Intron | NP_001034782.1 | |||
XM_017003310.1 | 258 | Intron | XP_016858799.1 |